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Lichenoid Drug Eruption Induced by Teriflunomide.

• Authors : Agharbi, Fatima-Zahra¹ ; Aasfara, Jehanne²; Oqbani, Kenza³

• Source: Annals of Indian Academy of Neurology. May/Jun2023, Vol. 26 Issue 3, p275-277. 3p.

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Clinico-Pathological Features in Köhlmeier--Degos Disease with Cutaneous and Neurological Involvement.

• Authors : Sindhu, Dodmallur Mallikarjuna¹; Shivaram, Sumanth¹; Rao, Shilpa²

• Source: Annals of Indian Academy of Neurology. Nov/Dec2021, Vol. 24 Issue 6, p1005-1009. 5p.

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Rare Cause of West syndrome secondary to Tubulinopathy due to Congenital Symmetric Circumferential Skin Creases (CSCSC) Kunze Type due to a Novel Variant in MAPRE2 Gene.

• Authors : Gowda, Vykuntaraju K.¹ ; Srinivasan, Varunvenkat M.²; Reddy, Varsha²

• Source: Annals of Indian Academy of Neurology. Mar/Apr2022, Vol. 25 Issue 2, p286-288. 3p.

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Lipoid proteinosis (urbach-wiethe disease): A rare genodermatosis with characteristic dermatological and neuroimaging findings.

• Authors : Chatterjee, Aparajita¹; Viswanathan, Lakshminarayanapuram¹; Nagappa, Madhu¹

• Source: Annals of Indian Academy of Neurology. Sep/Oct2021, Vol. 24 Issue 5, p761-762. 2p.

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Cutis Verticis Gyrata Heralding a Diagnosis of Primary Systemic Amyloidosis in a Patient with Cardioembolic Stroke.

• Authors : Agarwal, Ayush; Chatterpal, Pinki; Kant, Surya

Subjects: STROKE prevention; AMYLOIDOSIS diagnosis; THERAPEUTIC use of fibrinolytic agents

• Source: Annals of Indian Academy of Neurology; Jan/Feb2023, Vol. 26 Issue 1, p88-90, 3p

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What is new in idiopathic inflammatory myopathies: Mechanisms and therapies.

• Authors : Khadilkar, Satish; Dhamne, Megha

Subjects: BIOLOGICAL products; DERMATOMYOSITIS; HEART diseasesINDIA

• Source: Annals of Indian Academy of Neurology; Jul/Aug2020, Vol. 23 Issue 4, p458-467, 10p

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Urbach--Wiethe Disease: A Rare Cause of Bilateral Mesial Temporal Lobe Involvement and Cerebral Hemorrhage.

• Authors : Özdemir, Hüseyin Nezih¹ ; Çallı, Cem¹; Gökçay, Figen¹

• Source: Annals of Indian Academy of Neurology. May/Jun2022, Vol. 25 Issue 3, p526-527. 2p.

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Association of Incontinentia Pigmenti (Bloch-Sulzberger Syndrome) with Hereditary Motor Sensory Neuropathy: A case report.

• Authors : Joy, S. P.¹; Suresh, K.^2,3; Panda, S.^2,3

• Source: Annals of Indian Academy of Neurology. 2007 Supplement 2, Vol. 10, p51-51. 1/4p.

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